Canonical Allele Identifier: CA1619116305

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31353909A= , CM000668.2:g.31353909A=	GRCh38
NC_000006.11:g.31321686A= , CM000668.1:g.31321686A=	GRCh37
NC_000006.10:g.31429665A=	NCBI36
NG_023187.1:g.8304T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3528T=
ENST00000481849.6:n.3488T=
ENST00000497377.6:n.3395T=
ENST00000696558.1:c.1550T=	ENSP00000512716.1:n.1550T=
ENST00000696559.1:c.*392T=	ENSP00000512717.1:n.*392T=
ENST00000696560.1:c.*392T=	ENSP00000512718.1:n.*392T=
ENST00000696561.1:c.*392T=	ENSP00000512719.1:n.*392T=
ENST00000696562.1:c.*392T=	ENSP00000512720.1:n.*392T=
ENST00000412585.7:c.*392T= MANE Select	ENSP00000399168.2:n.*392T=
ENST00000412585.6:c.*392T=	ENSP00000399168.2:n.*392T=
ENST00000481849.5:n.716T=
ENST00000497377.5:n.880T=
NM_005514.6:c.*392T=	NP_005505.2:n.*392T=
XM_011514556.1:c.*392T=	XP_011512858.1:n.*392T=
XM_011514557.1:c.*392T=	XP_011512859.1:n.*392T=
XR_926175.1:n.1920T=
NM_005514.7:c.*392T=	NP_005505.2:n.*392T=
NM_005514.8:c.*392T= MANE Select	NP_005505.2:n.*392T=